无机材料学报 ›› 2011, Vol. 26 ›› Issue (6): 649-654.DOI: 10.3724/SP.J.1077.2011.00649

• 研究论文 • 上一篇    下一篇

(1-x)Pb(Fe2/3W1/3)O3-xPb(Mg1/2W1/2)O3多铁性材料的有序结构及磁性能

姚春发, 李财富, 刘志权, 尚建库   

  1. (中国科学院 金属研究所 沈阳材料科学国家(联合)实验室, 沈阳 110016)
  • 收稿日期:2010-08-30 修回日期:2010-12-03 出版日期:2011-06-20 网络出版日期:2011-06-07
  • 作者简介:姚春发(1985-), 男, 硕士研究生. E-mail: c.f.yao@163.com
  • 基金资助:

    国家重点基础研究发展计划973项目(2010CB631006);  中国科学院百人计划项目

Structural Ordering and Magnetic Property of Complex Perovskite Solid Solution (1-x)Pb(Fe2/3W1/3)O3-xPb(Mg1/2W1/2)O3

YAO Chun-Fa, LI Cai-Fu, LIU Zhi-Quan, SHANG Jian-Ku   

  1. (Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China)
  • Received:2010-08-30 Revised:2010-12-03 Published:2011-06-20 Online:2011-06-07
  • Supported by:

    National Basic Research Program of China (2010CB6310006); Hundred Talents Program of the Chinese Academy of Sciences

摘要: 以无机盐为前驱体, 利用溶胶?凝胶法固溶合成了(1-x)Pb(Fe2/3W1/3)O3-xPb(Mg1/2W1/2)O3多铁性固溶体. XRD分析表明, 在0≤x≤1.0的掺杂范围内, 700℃煅烧所得产物都具有钙钛矿结构; x=0时得到的纯Pb(Fe2/3W1/3)O3为长程无序结构, x=1.0时可获得完全有序的纯Pb(Mg1/2W1/2)O3相, 其单胞为Pb(Fe2/3W1/3)O3单胞的2倍; 当0<x<1.0时, (1-x)Pb(Fe2/3W1/3)O3-xPb(Mg1/2W1/2)O3固溶体也为有序结构, 出现1/2 (111)及1/2 (311) XRD衍射峰, 且强度随掺杂系数x的升高逐渐增大. TEM分析证实, 煅烧产物为具有钙钛矿结构的单相固溶体, 而非两相复合物; 固溶相形貌以立方颗粒为主, 随掺杂量增加其晶胞常数线性增大, 而晶粒尺寸先减小后变大. 性能测试发现, 固溶相的磁学性能随x的增加而逐渐下降, 起因于抗磁性的Pb(Mg1/2W1/2)O3破坏了Pb(Fe2/3W1/3)O3原有的价键结构所致.

关键词: 多铁性材料, 钙钛矿结构, 溶胶?凝胶, 固溶有序, 磁性能

Abstract: Pb(Fe2/3W1/3)O3 was modified by doping Pb(Mg1/2W1/2)O3 with Sol-Gel method using inorganic salts as precursors. At calcination temperature of 700℃, the resulted solid solution (1-x)Pb(Fe2/3W1/3)O3-xPb(Mg1/2W1/2)O3 kept a perovskite structure in the whole doping range of 0≤x≤1. The obtained Pb(Mg1/2W1/2)O3 (x=1) is fully ordered with a unit cell as two times as that of Pb(Fe2/3W1/3)O3 (x=0). Solid solution (1-x)Pb(Fe2/3W1/3)O3- xPb(Mg1/2W1/2)O3 (0<x<1.0) also has an ordered crystal structure showing supperlattice peaks of 1/2 (111) and 1/2 (311) in X-ray diffraction, whose intensities become stronger as x increases. Combining electron diffraction and elemental analysis in transmission electron microscope, solid solution (1-x)Pb(Fe2/3W1/3)O3-xPb(Mg1/2W1/2)O3 is verified as a single phase with perovskite structure, rather than a mixture of two phases. The particles of solid solution have a cubic morphology, and their grain size first decreases and then increases when doping coefficient x varies from 0.2 to 0.8. Due to the substitution of larger Mg2+ for smaller Fe3+ ions, its lattice constant increases linearly with the enhancement of x. According to the measured M-H curves, the magnetic performance of the solid solution decays as the doping coefficient x increases, because the formation of diamagnetic Pb(Mg1/2W1/2)O3 could destroy the -Fe3+-W-O-W-Fe3+- and -Fe3+-O-Fe3+- magnetic bonds in antiferromagnetic Pb(Fe2/3W1/3)O3 phase.

Key words: multiferroic, perovskite, Sol-Gel, ordering, magnetic property

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